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Links from Protein

Items: 3

1.
Metabolic and Chaperone Gene Loss Marks the Origin of Animals: Evidence for Hsp104 and Hsp78 Chaperones Sharing Mitochondrial Enzymes as Clients
Albert J. Erives, Jan S. Fassler
PLoS One. 2015; 10(2): e0117192. Published online 2015 Feb 24. doi: 10.1371/journal.pone.0117192
PMCID:
PMC4339202
AbstractArticlePDF–2.0M
2.
CLPB Mutations Cause 3-Methylglutaconic Aciduria, Progressive Brain Atrophy, Intellectual Disability, Congenital Neutropenia, Cataracts, Movement Disorder
Saskia B. Wortmann, Szymon Ziętkiewicz, Maria Kousi, Radek Szklarczyk, Tobias B. Haack, Søren W. Gersting, Ania C. Muntau, Aleksandar Rakovic, G. Herma Renkema, Richard J. Rodenburg, Tim M. Strom, Thomas Meitinger, M. Estela Rubio-Gozalbo, Elzbieta Chrusciel, Felix Distelmaier, Christelle Golzio, Joop H. Jansen, Clara van Karnebeek, Yolanda Lillquist, Thomas Lücke, Katrin Õunap, Riina Zordania, Joy Yaplito-Lee, Hans van Bokhoven, Johannes N. Spelbrink, Frédéric M. Vaz, Mia Pras-Raves, Rafal Ploski, Ewa Pronicka, Christine Klein, Michel A.A.P. Willemsen, Arjan P.M. de Brouwer, Holger Prokisch, Nicholas Katsanis, Ron A. Wevers
Am J Hum Genet. 2015 Feb 5; 96(2): 245–257. doi: 10.1016/j.ajhg.2014.12.013
PMCID:
PMC4320260
AbstractArticlePDF–1.3M
3.
CLPB Variants Associated with Autosomal-Recessive Mitochondrial Disorder with Cataract, Neutropenia, Epilepsy, and Methylglutaconic Aciduria
Carol Saunders, Laurie Smith, Flemming Wibrand, Kirstine Ravn, Peter Bross, Isabelle Thiffault, Mette Christensen, Andrea Atherton, Emily Farrow, Neil Miller, Stephen F. Kingsmore, Elsebet Ostergaard
Am J Hum Genet. 2015 Feb 5; 96(2): 258–265. doi: 10.1016/j.ajhg.2014.12.020
PMCID:
PMC4320254
AbstractArticlePDF–732K

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